DUTASTERIDE capsule, liquid filled

Dutasteride by

Drug Labeling and Warnings

Dutasteride by is a Prescription medication manufactured, distributed, or labeled by GlaxoSmithKline LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Storage and Handling

Store at 15-25°C

PRINCIPAL DISPLAY PANEL

NDC: 0173-7077-00

Dutasteride 0.5mg Capsules

Store at 15-25°C

Quantity 200 BLISTERS

INGREDIENTS AND APPEARANCE

DUTASTERIDE 
dutasteride capsule, liquid filled

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 0173-7077
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DUTASTERIDE (UNII: O0J6XJN02I) (DUTASTERIDE - UNII:O0J6XJN02I)	DUTASTERIDE	0.5 mg

Inactive Ingredients
Ingredient Name	Strength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
FERRIC OXIDE RED (UNII: 1K09F3G675)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL CAPRYLOCAPRATE (UNII: U72Q2I8C85)
WATER (UNII: 059QF0KO0R)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	RED	Score	no score
Shape	OVAL (soft gelatin capsule)	Size	19mm
Flavor		Imprint Code	GS;MUF
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0173-7077-00	20 in 1 CARTON	02/19/2015
1		10 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Export only		02/19/2015

Labeler - GlaxoSmithKline LLC (167380711)